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    The <em>General Information</em> section displays the SNP RS number, function, gene and
    gene aliases, a link to previous associations (if there are any), and
    links to LD plots for each cohort included in the study.
    The user can quickly navigate to the SNP summary page of another SNP
    by typing in its RS number in the "Search SNP" text box or by selecting
    another SNP in the current gene from the drop down menu. Links to
    information found on dbSNP, OMIM, and NCBI are provided here as well.
    <a href="http://www.ncbi.nlm.nih.gov/projects/SNP/" target="_blank">The Single Nucleotide Polymorphism database (dbSNPs)</a> is a public-domain
    archive for a broad collection of simple genetic polymorphisms and
    serves as a central public repository for genetic variation. <a href="http://www.ncbi.nlm.nih.gov/omim" target="_blank">The
    Online Mendelian Inheritance in Man (OMIM) database</a> is a catalog of
    human genes and genetic disorders and contains textual information,
    references and links to <a href="http://www.nlm.nih.gov/databases/databases_medline.html" target="_blank">MEDLINE</a>
    and sequence records in the <a href="http://www.ncbi.nlm.nih.gov/sites/gquery" target="_blank">Entrez system</a>
    as well as <a href="http://www.ncbi.nlm.nih.gov/" target="_blank">NCBI</a>. <a href="http://www.ncbi.nlm.nih.gov/sites/entrez" target="_blank">PubMed</a> is a service of the U.S. National
    Library of Medicine that includes millions of citations from MEDLINE
    and other life science journals as well as  links to full text articles
    and other related resources.
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